FDA.reportPublic FDA data

Grizzly Creek Naturals Hand Sanitizer

Manufacturer
BLACK BIRD POTENTIALS INC. | GRIZZLY CREEK FARMS, LLC
Effective date
2020-03-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:04:48

Label at a glance#

ProductGrizzly Creek Naturals Hand Sanitizer
Active ingredientISOPROPYL ALCOHOL
Label structure9 sections

Indications and uses

To decrease bacteria on the skin that could cause disease; Recommended for repeated use

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult super-vision. Use of product not recommended for infants.

Label contents#

Full prescribing information#

DRUG FACTS

OTC - ACTIVE INGREDIENT SECTION

Active ingredient Isopropyl Alcohol 99%

Purpose Antiseptic

DRUG FACTS

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Active ingredient Isopropyl Alcohol 99%

Purpose Antiseptic

Uses

OTC - PURPOSE SECTION

To decrease bacteria on the skin that could

cause disease; Recommended for repeated use

Warnings

WARNINGS SECTION

● For external use only: hands ● Flammable, keep away from fire or flame ● When using this product keep out of eyes. In

case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if irritation and redness develop or condition persists for more than 72 hours

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

OTC - WHEN USING SECTION

Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult super-vision. Use of product not recommended for infants.

Other information

OTHER SAFETY INFORMATION

Do not store above 105ºF. May discolor some fabrics. Harmful to wood finishes and plastics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, fragrance, aloe vera juice, sodium benzoate, potassium sorbate, xanthan gum.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult super-vision. Use of product not recommended for infants.

Uses

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin that could cause disease; Recommended for repeated use

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30 mL NDC: 73816-101- 30 mL label30 mL label01

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73816-101-012022-01-28C16284748780-1d6a99b39-bc42-a426-e053-dadaa90af4c2a1dce220-d4b0-3213-e053-2995a90a8262

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73816-101-01Grizzly Creek Naturals Hand Sanitizer30 mL in 1 BOTTLE, DISPENSINGLIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73816-101GRIZZLY CREEK NATURALS HAND SANITIZER (ALCOHOL) LIQUID [BLACK BIRD POTENTIALS INC.]1Legacy NDC, 1 package rows20200403_a1dce220-d4b0-3213-e053-2995a90a8262.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73816-10173816-101-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ISOPROPYL ALCOHOLND2M416302ACTIB
ALOE ARBORESCENS LEAF09TD8L5SQVIACT
XANTHAN GUMTTV12P4NEEIACT
WATER059QF0KO0RIACT
SODIUM BENZOATEOJ245FE5EUIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
VACCINIUM MYRTILLUS ANTHOCYANOSIDESR911H793SUIACT

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
a1dce220-d4b1-3213-e053-2995a90a8262a1dce220-d4b0-3213-e053-2995a90a82622020-03-27WarningsExact identifier
spl id: a1dce220-d4b1-3213-e053-2995a90a8262
spl set id: a1dce220-d4b0-3213-e053-2995a90a8262

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.